KAC-63 KNEE ARRAY COIL

KAC-63 KNEE ARRAY COIL is an FDA 510(k)-cleared medical device (K993898) manufactured by Mri Devices Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 3, 2000. Regulation: 8.